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This device conforms to the following standards:
EN 60601-1:2006/A1:2013: - General requirements for basic safety and essential performance
EN 60601-1-2:2015 - Medical Electrical Equipment - Electromagnetic compatibility - Requirements
and tests.
EN 60601-1-11:2010 - Medical Electrical Equipment - Requirements for medical electrical
equipment and medical electrical systems used in the home healthcare environment.
EN 1060-3:1997 + A2:2009 - Non-invasive sphygmomanometers - Supplementary requirements
for electromechanical blood pressure measuring systems.
EN 1060-4:2004 - Non-invasive sphygmomanometers - Test procedures to determine the overall
system accuracy of automated non-invasive sphygmomanometers.
This product conforms to the provisions of the EC Directive 93/42/EEC (Medical
Device Directive).
This product carries the CE mark and is manufactured in conformity with the RoHS
Directive 2011/65/EU.
MEDICAL ELECTRICAL EQUIPMENT needs special precautions regarding EMC.
For a detailed description of EMC requirements please contact an authorised local Service Centre
(see guarantee) or visit www.hot-europe.com/support..
Portable and mobile RF communications equipment can affect medical electrical equipment.
This product contains batteries and recyclable electronic waste. To protect the
environment, do not dispose of it in household waste, but take it to appropriate local
collection centre.
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